@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os130_head
{
this:
np:hasAssertion
dgn-np:NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os130_assertion
;
np:hasProvenance
dgn-np:NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os130_provenance
;
np:hasPublicationInfo
dgn-np:NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os130_assertion
a
np:Assertion
.
dgn-np:NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os130_provenance
a
np:Provenance
.
dgn-np:NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os130_assertion
{
miriam-gene:2475
a
ncit:C16612
.
lld:C0041341
a
ncit:C7057
.
dgn-gda:DGN8b64de66c5cc1222bb88d168e289e2a8
sio:SIO_000628
miriam-gene:2475
,
lld:C0041341
;
a
sio:SIO_001121
.
}
dgn-np:NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os130_provenance
{
dgn-np:NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os130_assertion
dcterms:description
"[Abnormal mammalian target of rapamycin (mTOR) complex signaling and defects in TSC1 and TSC2 have been associated with the development of subependymal giant cell astrocytomas (SEGAs) in tuberous sclerosis complex (TSC) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:21806479
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP422707.RAx9jpHDL52eUdZUe2R_G6QGo4O6kl0_pL0rhojAj23os130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:10+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}